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... to TH1-p.R202H). Whole brain extracts of  homozygous 
ICIEM Abstracts
ICIEM Abstracts
Th-ki/ki mice showed in the brain normal ...
... study, the methods to identify non-  homozygous 
Assessment of wheat variety stability using SSR markers
Assessment of wheat variety stability using SSR markers
Wang, Li Xin; Li, Hong Bo; Gu, Tie Cheng; Liu, Li Hua; Pang, Bin Shuang; Qiu, Jun; Zhao, Chang Ping
SSR loci and calculate the ...
... from TLR2 and TLR4. These individuals are  homozygous 
ESID 2014 ORAL PRESENTATIONS
ESID 2014 ORAL PRESENTATIONS
for a loss-of-function TIRAP allele. ...
... al. 2014). Fig. 1 The clamp 2 mutation is  homozygous 
The essential Drosophila CLAMP protein differentially regulates non-coding roX RNAs in male and females
The essential Drosophila CLAMP protein differentially regulates non-coding roX RNAs in male and females
Urban, Jennifer A.; Doherty, Caroline A.; Jordan, William T., III; Bliss, Jacob E.; Feng, Jessica; Soruco, Marcela M.; Rieder, Leila E.; Tsiarli, Maria A.; Larschan, Erica N.
lethal and the clamp 1 allele is ...
... and osteopenia were revealed in the  homozygous 
Standardized, systemic phenotypic analysis of Slc12a1I299F mutant mice
Standardized, systemic phenotypic analysis of Slc12a1I299F mutant mice
Kemter, Elisabeth; Rathkolb, Birgit; Becker, Lore; Bolle, Ines; Busch, Dirk H; Dalke, Claudia; Elvert, Ralf; Favor, Jack; Graw, Jochen; Hans, Wolfgang; Ivandic, Boris; Kalaydjiev, Svetoslav; Klopstock, Thomas; Rácz, Ildikó; Rozman, Jan; Schrewe, Anja; Schulz, Holger; Zimmer, Andreas; Fuchs, Helmut; Gailus-Durner, Valérie; de Angelis, Martin Hrabé; Wolf, Eckhard; Aigner, Bernhard
mutant mice which were also described in ...
... carried the silent mutation in the  homozygous 
Common silent mutations in all types of hereditary complement C1q deficiencies
Common silent mutations in all types of hereditary complement C1q deficiencies
Petry, Franz; Loos, Michael
(18%) or heterozygous (36%) state. ...
... (FVL) and prothrombin mutation (PTM).  Homozygous 
Homozygous factor V Leiden and double heterozygosity for factor V Leiden and prothrombin mutation
Homozygous factor V Leiden and double heterozygosity for factor V Leiden and prothrombin mutation
Saemundsson, Ymir; Sveinsdottir, Signý Vala; Svantesson, Henrik; Svensson, Peter J.
FVL and PTM have long been feared ...
... McDevitt 1989; Brodde 1991) in volunteers  homozygous 
β-Adrenoceptor polymorphisms
β-Adrenoceptor polymorphisms
Leineweber, K.; Büscher, R.; Bruck, H.; Brodde, O.-E.
for the Gly389 or Arg389 β1-adrenoceptors ...
... that leads to loss of dysbindin-1 in  homozygous 
Dysbindin-1 and Its Protein Family
Dysbindin-1 and Its Protein Family
Talbot, K.; Ong, W.- Y.; Blake, D. J.; Tang, J.; Louneva, N.; Carlson, G. C.; Arnold, S. E.
mice, which also shows a loss or reduction ...
... major microfibrillar proteins. The PDLs of  homozygous 
Dilated capillaries, disorganized collagen fibers and differential gene expression in periodontal ligaments of hypomorphic fibrillin-1 mice
Dilated capillaries, disorganized collagen fibers and differential gene expression in periodontal ligaments of hypomorphic fibrillin-1 mice
Ganburged, Ganjargal; Suda, Naoto; Saito, Masahiro; Yamazaki, Yosuke; Isokawa, Keitaro; Moriyama, Keiji
mgR mice showed one-quarter of the elastic ...
... CbCln3 wild-type, heterozygous, and  homozygous 
Membrane trafficking and mitochondrial abnormalities precede subunit c deposition in a cerebellar cell model of juvenile neuronal ceroid lipofuscinosis
Membrane trafficking and mitochondrial abnormalities precede subunit c deposition in a cerebellar cell model of juvenile neuronal ceroid lipofuscinosis
Fossale, Elisa; Wolf, Pavlina; Espinola, Janice A; Lubicz-Nawrocka, Tanya; Teed, Allison M; Gao, Hanlin; Rigamonti, Dorotea; Cattaneo, Elena; MacDonald, Marcy E; Cotman, Susan L
neuronal precursor cell lines, which can ...
... phenotypes and can be maintained via  homozygous 
Mouse Models of Receptor Tyrosine Kinases
Mouse Models of Receptor Tyrosine Kinases
Holcmann, Martin; Amberg, Nicole; Drobits, Barbara; Glitzner, Elisabeth; Komposch, Karin; Robson, Jonathan; Savarese, Fabio; Srivatsa, Sriram; Stulnig, Gabriel; Sibilia, Maria
breeding. ...
... PCCA c.425G > A(p. Gly142Asp) Founder  Homozygous 
Thirteen year retrospective review of the spectrum of inborn errors of metabolism presenting in a tertiary center in Saudi Arabia
Thirteen year retrospective review of the spectrum of inborn errors of metabolism presenting in a tertiary center in Saudi Arabia
Alfadhel, Majid; Benmeakel, Mohammed; Hossain, Mohammad Arif; Al Mutairi, Fuad; Al Othaim, Ali; Alfares, Ahmed A.; Al Balwi, Mohammed; Alzaben, Abdullah; Eyaid, Wafaa
, missense c.350G > A (p.Gly117Asp) ...
... the dominant gene “D” at the D locus: the  homozygous 
The genetics of colour in fat-tailed sheep: a review
The genetics of colour in fat-tailed sheep: a review
Lundie, Roger S.
recessive genotype “dd” giving the brown ...
... of the mutated GmKASIIIA gene. Lines  homozygous 
Mapping the low palmitate fap1 mutation and validation of its effects in soybean oil and agronomic traits in three soybean populations
Mapping the low palmitate fap1 mutation and validation of its effects in soybean oil and agronomic traits in three soybean populations
Cardinal, Andrea J.; Whetten, Rebecca; Wang, Sanbao; Auclair, Jérôme; Hyten, David; Cregan, Perry; Bachlava, Eleni; Gillman, Jason; Ramirez, Martha; Dewey, Ralph; Upchurch, Greg; Miranda, Lilian; Burton, Joseph W.
for the GmKASIIIA mutation (fap1) had a ...
... vs. CC), recessive model (CC + CT vs. TT),  homozygous 
Association between the MTHFR C677T polymorphism and risk of cancer: evidence from 446 case–control studies
Association between the MTHFR C677T polymorphism and risk of cancer: evidence from 446 case–control studies
Xie, Shu-Zhe; Liu, Zhi-Zhong; Yu, Jun-hua; Liu, Li; Wang, Wei; Xie, Dao-Lin; Qin, Jiang-Bo
model (TT vs. ...
... generated from mouse tissues bearing the  homozygous 
Autosomal recessive primary microcephaly (MCPH): clinical manifestations, genetic heterogeneity and mutation continuum
Autosomal recessive primary microcephaly (MCPH): clinical manifestations, genetic heterogeneity and mutation continuum
Mahmood, Saqib; Ahmad, Wasim; Hassan, Muhammad J
gene trap mutation display the cellular ...
... and enamelin in the ameloblasts in the  homozygous 
Rat wct mutation prevents differentiation of maturation-stage ameloblasts resulting in hypo-mineralization in incisor teeth
Rat wct mutation prevents differentiation of maturation-stage ameloblasts resulting in hypo-mineralization in incisor teeth
Osawa, Masaru; Kenmotsu, Shin; Masuyama, Taku; Taniguchi, Kazuyuki; Uchida, Takashi; Saito, Chikara; Ohshima, Hayato
teeth was the same as that in the ...
... CI = 1.03–1.12, P h < 0.001, I 2 = 54.2 %;  homozygous 
Association between the CYP1B1 polymorphisms and risk of cancer: a meta-analysis
Association between the CYP1B1 polymorphisms and risk of cancer: a meta-analysis
Liu, Jie-Ying; Yang, Yu; Liu, Zhi-Zhong; Xie, Jian-Jun; Du, Ya-Ping; Wang, Wei
model: OR = 1.09, 95 % CI = 1.02–1.17, P ...
... and impaired panicle development in the  homozygous 
Agrobacterium T-DNA insertion in the rice DWARF SHOOT AND DEFECTIVE PANICLE1 (DSDP1) gene causes a severe dwarf phenotype, reduces plant vigour, and affects seed germination
Agrobacterium T-DNA insertion in the rice DWARF SHOOT AND DEFECTIVE PANICLE1 (DSDP1) gene causes a severe dwarf phenotype, reduces plant vigour, and affects seed germination
Basu, Debjani; Majhi, Bharat Bhusan; Sripriya, Rajasekaran; Veluthambi, Karuppannan
state. ...
... compromise juvenile survival. A scan for  homozygous 
A missense mutation in TUBD1 is associated with high juvenile mortality in Braunvieh and Fleckvieh cattle
A missense mutation in TUBD1 is associated with high juvenile mortality in Braunvieh and Fleckvieh cattle
Schwarzenbacher, Hermann; Burgstaller, Johann; Seefried, Franz R.; Wurmser, Christine; Hilbe, Monika; Jung, Simone; Fuerst, Christian; Dinhopl, Nora; Weissenböck, Herbert; Fuerst-Waltl, Birgit; Dolezal, Marlies; Winkler, Reinhard; Grueter, Oskar; Bleul, Ulrich; Wittek, Thomas; Fries, Ruedi; Pausch, Hubert
haplotype deficiency revealed a short ...
... of homozygotes. Results A scan for  homozygous 
Homozygous haplotype deficiency reveals deleterious mutations compromising reproductive and rearing success in cattle
Homozygous haplotype deficiency reveals deleterious mutations compromising reproductive and rearing success in cattle
Pausch, Hubert; Schwarzenbacher, Hermann; Burgstaller, Johann; Flisikowski, Krzysztof; Wurmser, Christine; Jansen, Sandra; Jung, Simone; Schnieke, Angelika; Wittek, Thomas; Fries, Ruedi
haplotype deficiency in 25,544 Fleckvieh ...
... test, the exploratory activity of the  homozygous 
Targeted mutation of CCK2 receptor gene modifies the behavioural effects of diazepam in female mice
Targeted mutation of CCK2 receptor gene modifies the behavioural effects of diazepam in female mice
Raud, Sirli; Rünkorg, Kertu; Veraksitš, Alar; Reimets, Ain; Nelovkov, Aleksei; Abramov, Urho; Matsui, Toshimitsu; Bourin, Michel; Volke, Vallo; Kõks, Sulev; Vasar, Eero
(−/−) mice was significantly higher ...
... extremely unfit to reproduce. In addition,  homozygous 
Poor competitive fitness of transgenically mitigated tobacco in competition with the wild type in a replacement series
Poor competitive fitness of transgenically mitigated tobacco in competition with the wild type in a replacement series
Al-Ahmad, Hani; Galili, Shmuel; Gressel, Jonathan
TM progeny had an even lower competitive ...
... Bonferroni correction (RANKL, rs4531631:  homozygous 
Association Between Single Nucleotide Polymorphisms in NFATC1 Signaling Pathway Genes and Susceptibility to Congenital Heart Disease in the Chinese Population
Association Between Single Nucleotide Polymorphisms in NFATC1 Signaling Pathway Genes and Susceptibility to Congenital Heart Disease in the Chinese Population
Wang, Fengyu; Wang, Haili; Wang, Lina; Zhou, Shiyuan; Chang, Mingxiu; Zhou, Jiping; Dou, Yongheng; Wang, Yanli; Shi, Xiangdong
, AA vs. ...